Classifications

• • H—ELECTRICITY
  • H01—ELECTRIC ELEMENTS
  • H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
  • H01J63/00—Cathode-ray or electron-stream lamps
  • H01J63/02—Details, e.g. electrode, gas filling, shape of vessel
  • H01J63/04—Vessels provided with luminescent coatings; Selection of materials for the coatings
• • C—CHEMISTRY; METALLURGY
  • C03—GLASS; MINERAL OR SLAG WOOL
  • C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
  • C03C3/00—Glass compositions
  • C03C3/04—Glass compositions containing silica
  • C03C3/076—Glass compositions containing silica with 40% to 90% silica, by weight
  • C03C3/095—Glass compositions containing silica with 40% to 90% silica, by weight containing rare earths
• • C—CHEMISTRY; METALLURGY
  • C03—GLASS; MINERAL OR SLAG WOOL
  • C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
  • C03C3/00—Glass compositions
  • C03C3/12—Silica-free oxide glass compositions
  • C03C3/14—Silica-free oxide glass compositions containing boron
  • C03C3/15—Silica-free oxide glass compositions containing boron containing rare earths
• • C—CHEMISTRY; METALLURGY
  • C03—GLASS; MINERAL OR SLAG WOOL
  • C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
  • C03C4/00—Compositions for glass with special properties
  • C03C4/12—Compositions for glass with special properties for luminescent glass; for fluorescent glass

Definitions

• the invention relates to a luminescent alumino-silicate and/or alumino-borate glass comprising lanthanum and/or gadolinium and activated by a rare earth metal.
• the invention also relates to a luminescent screen provided with such a glass.
• Luminescent glasses of the type described above are known from U.S. Pat. No. 4,102,805, describing luminescent alumino-silicate glasses activated by bivalent europium and also comprising a further oxide, for example, lanthanum oxide.
• the Japanese patent application No. 74-99610 laid open to public inspection, describes luminescent silicate and/or borate glasses activated by trivalent terbium and trivalent europium, which comprise one or more of the oxides of aluminium, lanthanum and the alkaline earth metals and furthermore an alkali metal oxide.
• a drawback of the known luminescent glasses is that they generally have a low efficiency. Particularly the quantum efficiency upon excitation by ultraviolet radiation is often found to be a factor of 5 to 10 smaller than the quantum efficiencies which can be achieved with efficient crystalline materials.
• a further drawback of the alkali-metal containing luminescent glasses is that they generally have a large decline in the luminous flux in practical uses, for example, in discharge lamps.
• Luminescent alumino-borate and/or alumino-silicate glasses activated by Tb 3+ and/or Ce 3+ and comprising one or more alkaline earth metal oxides are known from Netherlands patent application No. 58501107 (PHN 11.363).
• a luminescent alumino-silicate and/or alumino-borate glass comprising lanthanum and/or gadolinium and activated by a rare earth metal
• the glass is activated by at least one of the rare earth metals Tb 3+ and Ce 3+ and has a composition comprising 35-85 mol% of SiO 2 and/or B 2 O 3 , 1-35 mol% of La 2 O 3 and/or Gd 2 O 3 , 5-45 mol% of Al 2 O 3 and 0.5-30 mol% of Tb 2 O 3 and/or Ce 2 O 3 , in which the La 2 O 3 and/or Gd 2 O 3 may be replaced up to not more than 50 mol% by one or more of the oxides Y 2 O 3 , Sc 2 O 3 , Lu 2 O 3 , Zr ZrO 2 , P 2 O 5 and the alkaline earth metal oxides.
• glasses having a composition in the range mentioned above constitute very efficiently luminescing materials.
• glasses Upon activation by terbium, glasses are obtained having the characteristic green Tb 3+ -emission (maximum at approximately 540 nm) and upon activation by cerium an emission is obtained in a band in the blue or near ultraviolet part of the spectrum.
• Ce and Tb there is transfer of excitation energy from the Ce to the Tb.
• quantum efficiencies of 80% and more are possible upon UV-excitation.
• the glass matrix (that is to say, the glass composition without the activator oxide Tb 2 O 3 and/or Ce 2 O 3 ) is transparent to the exciting ultraviolet radiation.
• Useful absorption of the exciting ultraviolet radiation takes place in the activators Tb 3+ and/or Ce 3+ .
• the Tb 2 O 3 content may be chosen to be relatively high.
• Tb 2 O 3 contents of less than 0.5 mol% too low luminous fluxes are obtained because then the absorption of ultraviolet radiation is too small.
• Tb 2 O 3 contents of more than 30 mol% are not used because then too low luminous fluxes are obtained due to concentration quenching on the one hand and the glass formation is very difficult or impossible on the other hand.
• the Ce 2 O 3 content is chosen to be not smaller than 0.5 mol% for the same reason as for Tb 3+ .
• the upper limit of the Ce 2 O 3 content will be approximately 5 mol% in practice because undesired formation of Ce 4+ can hardly be avoided in the case of higher concentrations.
• the composition of the luminescent glass according to the invention is to be chosen within the above defined range, because it has been found that glass formation is not very well possible outside this range due to a too high melting temperature and/or due to inevitable crystallisation of the glass. It was found that, as far as the glass formation permits, the La 2 O 3 and/or Gd 2 O 3 can be replaced without any objection, up to not more than 50 mol% by one or more of the oxides Y 2 O 3 , Sc 2 O 3 , Lu 2 O 3 , ZrO 2 , P 2 O 5 and the alkaline earth metals which do not have a disturbing UV absorption. Alkaline earth metals in this description and the Claims are understood to be the elements Mg, Ca, Sr, Ba and Zn.
• the luminescent glasses according to the invention can be used instead of crystalline luminescent materials in, for example, discharge lamps. They then have great advantages with respect to crystalline materials. For example, there is a greater possibility of variation in the composition so that optimization of the luminescent properties is better possible.
• the glasses also have their specific favourable possibilities of processing and design.
• the glass may be used in, for example, luminescent glass fibres.
• the luminescent glasses according to the invention can also be used advantageously in cathode ray tubes and in solid state lasers.
• a luminescent glass according to the invention which is characterized in that the glass comprises 50-80 mol% of SiO 2 and/or B 2 O 3 , 1-20 mol% of La 2 O 3 , 10-30 mol% of Al 2 O 3 and 0.5-15 mol% of Tb 2 O 3 and/or Ce 2 O 3 .
• the glass formation proceeds most easily and that the highest quantum efficiencies are obtained.
• the luminescent glasses are preferably used in a luminescent screen which has a luminescent layer comprising the luminescent glass according to the invention and which layer can be provided on a support.
• a luminescent screen which has a luminescent layer comprising the luminescent glass according to the invention and which layer can be provided on a support.
• Such screens are used in, for example, discharge lamps, preferably low-pressure mercury vapour discharge lamps.
• the luminescent glasses according to the invention can be obtained by heating a starting mixture of the composite oxides, or of compounds yielding these oxides at an elevated temperature, to a high temperature in a furnace until at least the melting point is reached.
• the melting point is generally in the range between 1000 ° and 1800° C., dependent on the composition.
• the heat treatment is preferably carried out in a weakly reducing atmosphere in order to obtain or maintain the terbium and/or cerium in the trivalent state.
• the melt is maintained at a high temperature for some time, which leads to homogenization, and is subsequently cooled.
• This mixture of starting materials all having a high degree of purity (at least 99.99% for the rare earth metal oxides and at least 99.999% for the other oxides) was heated to 1200° C. in an aluminium oxide crucible in a furnace.
• the molten mixture was maintained at this temperature for 1 hour.
• a weakly reducing gas nitrogen with approximately 5% by volume of hydrogen
• the melt was quickly cooled by pouring in a carbon mold.
• the luminescent Tb 3+ -activated glass obtained was broken and subjected to a grinding treatment, whereafter the pulverulent product was ready for use.
• a number of glasses according to the invention activated by Ce 3+ or by Ce 3+ and Tb 3+ was prepared in an analogous manner as described in Example 1. All glasses were melted in aluminium oxide crucibles at 1200° C. in a weakly reducing atmosphere.
• the following Table shows the compositions and also the quantum efficiencies q (in %) upon excitation by 254 nm radiation as well as the absorption A (in %) of the exciting radiation.
• the glass activated by Ce 3+ only had an emission in a band with a maximum at approximately 375 nm. In the glasses activated by Ce 3+ and Tb 3+ a transfer of excitation energy was effectively realized from the Ce to the Tb and the characteristic Tb 3+ emission was obtained with these glasses.

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• Chemical & Material Sciences (AREA)
• Life Sciences & Earth Sciences (AREA)
• Engineering & Computer Science (AREA)
• Chemical Kinetics & Catalysis (AREA)
• General Chemical & Material Sciences (AREA)
• Geochemistry & Mineralogy (AREA)
• Materials Engineering (AREA)
• Organic Chemistry (AREA)
• Glass Compositions (AREA)
• Luminescent Compositions (AREA)
• Vessels And Coating Films For Discharge Lamps (AREA)

Applications Claiming Priority (2)

Publications (1)

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Cited By (27)

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Citations (4)

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• 1986
  • 1986-10-08 NL NL8602518A patent/NL8602518A/nl not_active Application Discontinuation
• 1987
  • 1987-10-05 EP EP87201899A patent/EP0266812B1/fr not_active Expired
  • 1987-10-05 JP JP62250038A patent/JPS63100039A/ja active Pending
  • 1987-10-05 DE DE8787201899T patent/DE3770582D1/de not_active Expired - Lifetime
  • 1987-10-07 US US07/105,921 patent/US4798768A/en not_active Expired - Fee Related

Patent Citations (4)

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